The National Rosacea Society (NRS) is sustained primarily by donations from individuals and industry. Donations from individuals are used to support the research grants program unless otherwise designated by the donors. Donations from industry are used to support public awareness and educational program services, and the NRS is solely responsible for the development and content of materials. All health information is reviewed by independent physician experts to ensure accuracy, noncommercial integrity and respect for medical science.
The most recent Form 990 by the National Rosacea Society may be viewed here (PDF).
The National Rosacea Society is a 501(c)(3) nonprofit organization whose mission is to improve the lives of people with rosacea by raising awareness, providing public health information and supporting medical research on this widespread but little-known disorder. The information the Society provides should not be considered medical advice, nor is it intended to replace
consultation with a qualified physician. The Society does not evaluate, endorse or recommend any particular medications, products, equipment or treatments. Rosacea may vary substantially from one patient to another, and treatment must be tailored by a physician for each individual case. For more information, visit About Us.